Brimonidine Eye Drops for Treatment of Ocular Graft-vs-Host Disease (oGVHD)

Stopped early · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Dry Eye, Ocular Graft vs Host Disease, Meibomian Gland Dysfunction

In brief

The objective of this study is to establish whether patients with dry eye disease (DED) are able to tolerate receiving Brimonidine: 0.15% eye drops two times a day for twelve weeks (primary tolerability objective) and to investigate the preliminary efficacy of Brimonidine 0.15% topical eye drop solution in treating Meibomian Gland Dysfunction (MGD) (primary efficacy objective). Meibomian Gland dysfunction can happen with numerous conditions such as Rosacea, Sjögren's syndrome, and oGVHD. In order to limit the influence of differing etiologies on the outcome of this trial, the investigator has limited the screening to MGD that accompanies oGVHD.

Key facts

Study ID

NCT02975557

Run by

Sandeep Jain, MD

People needed

15

Starts

2016-05-01

Expected to finish

2017-04-13

Last updated by the study team

2019-11-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Aged 18 years or older.
• Capable of giving informed consent and does provide informed consent.
• Diagnosis of Meibomian Gland Disease
• Women must be post-menopausal ≥ 1 year, or surgically sterilized. If not, a negative urine pregnancy test is required within 7 days of the participant receiving first dose of study drug along with definite evidence of contraceptive use during the duration of the study. Women of reproductive age should use a method of birth control that is acceptable to the participant and the study doctor. This may include oral contraceptive pills, birth control implants, barrier methods or abstinence. If a participant suspects pregnancy after being enrolled, another pregnancy test will be administered. If the test is positive, the participant will be discontinued from the study immediately.

You may not qualify if…

• Allergic to Brimonidine or any similar products, or excipients of Brimonidine
• Currently receiving any Brimonidine preparation as a part of glaucoma management
• Receiving or have received within 30 days any experimental systemic medication.
• Active ocular infection or ocular allergies.
• Any history of eyelid surgery or ocular surgery within the past 3 months.
• Corneal epithelial defect larger than 1 mm2 in either eye.
• Have active drug/alcohol dependence or abuse history.
• Vulnerable populations, such as neonates, pregnant women, children, prisoners, institutionalized individuals, or others who may be considered vulnerable populations.

Where it is running

• Illinois Eye and Ear Infirmary, University of Illinois — Chicago, Illinois, United States
• Translational Clinic of Corneal Neurobiology Laboratory, Illinois Eye and Ear Infirmary, University of Illinois — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.